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首页> 外文期刊>Molecular biology reports >Inter and intra-ethnic differences in the distribution of the molecular variants of TPMT, UGT1A1 and MDR1 genes in the South Indian population
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Inter and intra-ethnic differences in the distribution of the molecular variants of TPMT, UGT1A1 and MDR1 genes in the South Indian population

机译:TPMT,UGT1A1和MDR1基因的分子变异在南印度人口中的种族间和种族内差异

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摘要

Molecular variants of polymorphic drug metabolizing enzymes and drug transporters are attributed to differences in individual's therapeutic response and drug toxicity in different populations. We sought to determine the genotype and allele frequencies of polymorphisms for major phase II drug-metabolizing enzymes (TPMT, UGT1A1) and drug transporter (MDR1) in South Indians. Allelic variants of TPMT (*2,*3A,*3B,*3C & *8), UGT1A1 (TA)6 > 7 and MDR1 (2677G > T/A & 3435C > T) were evaluated in 450-608 healthy South Indian subjects. Genomic DNA was extracted by phenol-chloroform method and genotype was determined by PCR-RFLP, qRT-PCR, allele specific PCR, direct sequencing and SNaPshot techniques. The frequency distributions of TPMT, UGT1A1 and MDR1 gene polymorphisms were compared between the individual 4 South Indian populations viz., Tamilian, Kannadiga, Andhrite and Keralite. The combined frequency distribution of the South Indian populations together, was also compared with that of other major populations. The allele frequencies of TPMT*3C, UGT1A1 (TA)7, MDR1 2677T, 2677A and 3435T were 1.2, 39.8, 60.3, 3.7, and 61.6% respectively. The other variant alleles such as TPMT*2, *3A, *3B and *8 were not identified in the South Indian population. Sub-population analysis showed that the distribution of UGT1A1 (TA)6 > 7 and MDR1 allelic variants differed between the four ethnic groups. However, the frequencies of TPMT*3C allele were similar in the four South Indian populations. The distribution of TPMT, UGT1A1 and MDR1 gene polymorphisms of the South Indian population was significantly different from other populations.
机译:多态性药物代谢酶和药物转运蛋白的分子变异归因于不同人群中个体的治疗反应和药物毒性的差异。我们试图确定南印度人主要II期药物代谢酶(TPMT,UGT1A1)和药物转运蛋白(MDR1)的多态性的基因型和等位基因频率。在450-608健康的南印度人中评估了TPMT(* 2,* 3A,* 3B,* 3C&* 8),UGT1A1(TA)6> 7和MDR1(2677G> T / A&3435C> T)的等位基因变体科目。通过酚-氯仿法提取基因组DNA,并通过PCR-RFLP,qRT-PCR,等位基因特异性PCR,直接测序和SNaPshot技术确定基因型。比较了印度南部4个人口中TPMT,UGT1A1和MDR1基因多态性的频率分布,这些人口分别是泰米尔人,卡纳迪加人,安德莱特人和方钠石人。还将南印度人口的合并频率分布与其他主要人口的频率分布进行了比较。 TPMT * 3C,UGT1A1(TA)7,MDR1 2677T,2677A和3435T的等位基因频率分别为1.2、39.8、60.3、3.7和61.6%。在南印度人口中未发现其他变异等位基因,如TPMT * 2,* 3A,* 3B和* 8。亚群分析显示,四个种族之间的UGT1A1(TA)6> 7和MDR1等位基因变异体的分布有所不同。但是,TPMT * 3C等位基因的频率在四个南印度人口中相似。南印度人口的TPMT,UGT1A1和MDR1基因多态性的分布与其他人口明显不同。

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